Abstract | OBJECTIVE: To isolate and identify the genotype and molecular characteristic of an imported D9 measles virus. METHOD: To isolate the virus with Vero/SLAM cell line. And RT-PCR (reverse transcription-polymerase chain reaction) were performed to amplify the 450 nucleotide acids of carboxyl terminal of N ( nucleoprotein, N) protein. The phylogenetic tree was constructed and the homology similarity was analyzed. RESULTS: Sichuan isolate MVi/Sichuan.CHN/07.09/1 was clustered within the same genotype group with WHO D9 genotype reference strain, the homology of nucleotide acid between Sichuan isolate and WHO D9 genotype reference strain was 96.9%. The homology of nucleotide acid and amino acid between Sichuan isolate and 2008 D9 genotype representative strain were 99.8%-100% and 99.3%-100% respectively. Compared with the Chinese measles vaccine strain, the homology of nucleotide acid and amino acid of Shanghai-191 were 92.3% and 90.7% respectively. Compared with the endemic H1 genotype representative measles strain, the homology of nucleotide acid and amino acid were 90.8% and 92.1% respectively. CONCLUSION: The imported virus was D9 genotype measles virus.
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Authors | Yan Zhang, Ji-Lan He, Li Sun |
Journal | Zhongguo yi miao he mian yi
(Zhongguo Yi Miao He Mian Yi)
Vol. 15
Issue 4
Pg. 304-9
(Aug 2009)
ISSN: 1006-916X [Print] China |
PMID | 20077726
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Topics |
- Animals
- China
- Chlorocebus aethiops
- Female
- Genotype
- Humans
- Measles
(virology)
- Measles virus
(classification, genetics, isolation & purification)
- Molecular Sequence Data
- Phylogeny
- Travel
- Vero Cells
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